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BMRN Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
54.880
Open
53.200
VWAP
54.29
Vol
632.95K
Mkt Cap
10.31B
Low
53.180
Amount
34.37M
EV/EBITDA(TTM)
11.17
Total Shares
193.28M
EV
9.51B
EV/OCF(TTM)
10.88
P/S(TTM)
3.20
BioMarin Pharmaceutical Inc. is a global biotechnology company engaged in the development of genetic discovery into medicines that make an impact on the life of each patient. The Company has a portfolio of commercial therapies and a clinical and preclinical pipeline. Its commercial products include Vimizim (elosulfase alpha), Naglazyme (galsulfase), Palynziq (pegvaliase-pqpz), Brineura (cerliponase alfa), Aldurazyme (laronidase), Roctavian (valoctocogene roxaparvovec), Kuvan (sapropterin dihydrochloride), and Voxzogo (vosoritide). Vimizim is an enzyme replacement therapy for the treatment of MPS IVA, a lysosomal storage disorder. The Roctavian is an adeno-associated virus (AAV5) vector gene therapy designed to restore factor VIII plasma concentrations in patients with severe hemophilia A. Its Galafold (migalastat) is the first oral treatment for Fabry disease, and Pombiliti (cipaglucosidase alfa-atga) + Opfolda (miglustat), is a two-component therapy for Pompe disease.
Show More

Events Timeline

(ET)
2026-05-20
16:30:00
BioMarin Announces Successful Voxzogo Clinical Trial
select
2026-05-18 (ET)
2026-05-18
09:10:00
BioMarin Announces Results of BMN 401 Trial
select

News

CNBC
8.0
05-29CNBC
Morgan Stanley Bullish on Dividend Stocks
  • Dividend Potential Analysis: Morgan Stanley highlights that companies initiating dividends outperform the market by an average of 650 basis points in the six months following the announcement and by 1,000 basis points in the subsequent 12 months, indicating a significant enhancement in investor returns, especially when dividends are reinvested for compounding benefits.
  • Centene's Advantages: Centene boasts an 18% free cash flow yield and a net cash position exceeding 5% of its market cap, making it an ideal candidate for dividends; additionally, the company surpassed expectations for adjusted earnings per share and revenue in Q1, with its stock rising 44% this year.
  • BioMarin's Acquisition Impact: BioMarin, with a net cash position of 7.6% of its market cap and a 10.4% free cash flow yield, successfully made the list after completing a $4.8 billion acquisition of Amicus Therapeutics, which is expected to significantly enhance its market share in rare metabolic diseases, although it slightly lowered its 2026 non-GAAP earnings per share guidance while raising its full-year revenue guidance to $3.825 to $3.925 billion.
  • Deckers Outdoor's Growth Outlook: Deckers Outdoor posted better-than-expected results for its fiscal Q1, with a free cash flow yield of 6.7%, and analysts have rated the stock as a buy, anticipating that its portfolio of category-defining brands will drive future growth, with shares gaining nearly 10% this year.
seekingalpha
9.0
05-20seekingalpha
BioMarin's Voxzogo Phase 3 Data Shows Positive Results
  • Clinical Trial Success: BioMarin Pharmaceutical's phase 3 trial for Voxzogo (vosoritide) in children with hypochondroplasia met its primary endpoint, demonstrating a statistically significant increase in annualized growth velocity compared to the placebo group.
  • Significant Height Increases: Children treated with Voxzogo showed notable improvements in standing height and height Z-scores after one year, indicating the drug's effectiveness in promoting growth in pediatric patients.
  • Accelerated Approval Context: Voxzogo received accelerated approval in November 2021, necessitating a post-market study to confirm its efficacy and ensure its continued availability in the market.
  • Future Plans: BioMarin intends to submit a supplemental New Drug Application (sNDA) to the US FDA in Q3 to seek full approval for Voxzogo, further solidifying its market position.
PRnewswire
8.5
05-20PRnewswire
BioMarin's VOXZOGO Study Achieves Significant Growth Milestones
  • Clinical Trial Success: BioMarin's VOXZOGO Phase 3 study for children with hypochondroplasia achieved a statistically significant annualized growth velocity (AGV) increase of 2.33 cm/year compared to placebo at week 52 (p<0.0001), providing new hope for treatment options.
  • Height and Arm Span Improvements: Children receiving VOXZOGO also demonstrated significant increases in standing height and height Z-score (p<0.0001), which not only enhances their daily functioning but may also improve their independence.
  • Consistent Safety Profile: The safety findings for VOXZOGO were consistent with its established profile in achondroplasia, with no new safety signals identified, thereby supporting the drug's further development and market introduction.
  • Regulatory Submission Plans: BioMarin plans to submit a supplemental New Drug Application (sNDA) to the FDA in Q3 2026, followed by submissions to the EMA and other regional health authorities, indicating a strategic push into global markets.
Newsfilter
9.0
05-20Newsfilter
BioMarin's VOXZOGO Study Achieves Significant Growth Milestones
  • Clinical Trial Success: BioMarin's VOXZOGO achieved a statistically significant increase in annualized growth velocity (AGV) of 2.33 cm/year compared to placebo in its Phase 3 study for children with hypochondroplasia, exceeding expectations and indicating the drug's potential to improve growth outcomes.
  • Height and Arm Span Improvements: The study demonstrated significant increases in standing height and height Z-score for children receiving VOXZOGO, suggesting potential enhancements in daily activities and independence for these patients.
  • Safety Profile Confirmed: The safety findings for VOXZOGO were consistent with the established profile in achondroplasia, with no new safety signals identified, thereby reinforcing confidence in its use for treating hypochondroplasia.
  • Regulatory Submission Plans: BioMarin plans to submit a supplemental New Drug Application (sNDA) to the FDA in Q3 2026, followed by submissions to the EMA and other regional health authorities, marking a critical step towards market availability.
seekingalpha
9.0
05-18seekingalpha
BioMarin's BMN 401 Phase 3 Trial Results Mixed
  • Trial Results: BioMarin's BMN 401 phase 3 trial for ENPP1 deficiency achieved only one of its two primary endpoints, with significant increases in plasma PPi levels over 52 weeks compared to the control group, but failed to meet the improvement in Radiographic Global Impression of Change (RGI-C), potentially impacting its market viability.
  • Secondary Endpoints Missed: No positive trends were observed in secondary endpoints such as Rickets Severity Score (RSS) and growth Z-score, indicating limited efficacy of BMN 401, which may undermine investor confidence and future funding opportunities.
  • Data Analysis Next Steps: BioMarin is currently analyzing the trial data to determine subsequent actions, a process that could influence its future research directions and resource allocation, particularly in the rare disease sector.
  • Background on ENPP1 Deficiency: ENPP1 deficiency is a genetic condition leading to low pyrophosphate levels, and while BioMarin aims to address this medical gap, the complexity of the trial results may delay the product's market entry.
PRnewswire
9.0
05-18PRnewswire
BioMarin's ENERGY 3 Study Results on ENPP1 Deficiency
  • Clinical Trial Results: BioMarin's ENERGY 3 trial demonstrated that treatment with BMN 401 led to statistically significant increases in plasma inorganic pyrophosphate (PPi) levels in children with ENPP1 deficiency over 52 weeks; however, no improvement was observed in Radiographic Global Impression of Change (RGI-C) scores, indicating limited treatment efficacy.
  • Safety Assessment: BMN 401 was generally well-tolerated during the trial with no new safety signals reported, yet no positive trends were noted across secondary endpoints, including Rickets Severity Score and growth Z-score, highlighting the treatment's limitations.
  • Significance of the Study: ENPP1 deficiency is a severe genetic condition with high mortality rates in infants, reaching up to 50%, thus the lack of significant clinical improvement from BMN 401 underscores the urgent need for new treatment options in this area.
  • Next Steps: BioMarin is actively evaluating the trial data to determine the appropriate next steps for BMN 401, with plans to present detailed results at an upcoming medical meeting, continuing to focus on advancements in this critical research area.
Wall Street analysts forecast BMRN stock price to rise
19 Analyst Rating
Wall Street analysts forecast BMRN stock price to rise
14 Buy
5 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
60.00
Averages
87.35
High
120.00
Current: 0.000
sliders
Low
60.00
Averages
87.35
High
120.00
BofA
Jason Zemansky
Buy
maintain
$85 -> $80
AI Analysis
2026-05-19
Reason
BofA
Jason Zemansky
Price Target
$85 -> $80
AI Analysis
2026-05-19
maintain
Buy
Reason
BofA analyst Jason Zemansky lowered the firm's price target on BioMarin to $80 from $85 and keeps a Buy rating on the shares after the company announced the Phase 3 topline results for BMN401 in ENPP1 deficiency with mixed results on the co-primary endpoints. Given a lack of corresponding clinical improvement despite biomarker benefit, the firm thinks it is prudent to remove its risk-adjusted BMN401 forecast from its model, which reduces its price target and trims its 2027-28 topline and EPS forecast by 1%, the analyst tells investors.
Citi
Buy
initiated
$75
2026-05-18
Reason
Citi
Price Target
$75
2026-05-18
initiated
Buy
Reason
Citi initiated coverage of BioMarin with a Buy rating and $75 price target. The firm views the stock's "dislocated" valuation as a product of "overly cautious" views on Voxzogo's competitive exposure. Citi sees the shares rallying over the medium term on visibility into the Amicus business.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for BMRN
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Valuation Metrics

The current forward P/E ratio for BioMarin Pharmaceutical Inc (BMRN.O) is 11.05, compared to its 5-year average forward P/E of 34.45. For a more detailed relative valuation and DCF analysis to assess BioMarin Pharmaceutical Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PE
34.45
Current PE
11.05
Overvalued PE
57.79
Undervalued PE
11.11

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average EV/EBITDA
36.19
Current EV/EBITDA
11.23
Overvalued EV/EBITDA
64.52
Undervalued EV/EBITDA
7.86

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
5.70
Current PS
2.38
Overvalued PS
7.54
Undervalued PS
3.86

Financials

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Whales Holding BMRN

C
Caxton Associates (USA) LLC
Holding
BMRN
+32.19%
3M Return
B
Bluebox Asset Management Uk Ltd.
Holding
BMRN
+28.97%
3M Return
P
PRIMECAP Management Company
Holding
BMRN
+27.67%
3M Return
B
Braidwell LP
Holding
BMRN
+11.87%
3M Return
N
Novo Holdings A/S
Holding
BMRN
+9.78%
3M Return
V
Viking Global Investors LP
Holding
BMRN
+7.22%
3M Return

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Frequently Asked Questions

What is BioMarin Pharmaceutical Inc (BMRN) stock price today?

The current price of BMRN is 54.82 USD — it has increased 2.81

What is BioMarin Pharmaceutical Inc (BMRN)'s business?

BioMarin Pharmaceutical Inc. is a global biotechnology company engaged in the development of genetic discovery into medicines that make an impact on the life of each patient. The Company has a portfolio of commercial therapies and a clinical and preclinical pipeline. Its commercial products include Vimizim (elosulfase alpha), Naglazyme (galsulfase), Palynziq (pegvaliase-pqpz), Brineura (cerliponase alfa), Aldurazyme (laronidase), Roctavian (valoctocogene roxaparvovec), Kuvan (sapropterin dihydrochloride), and Voxzogo (vosoritide). Vimizim is an enzyme replacement therapy for the treatment of MPS IVA, a lysosomal storage disorder. The Roctavian is an adeno-associated virus (AAV5) vector gene therapy designed to restore factor VIII plasma concentrations in patients with severe hemophilia A. Its Galafold (migalastat) is the first oral treatment for Fabry disease, and Pombiliti (cipaglucosidase alfa-atga) + Opfolda (miglustat), is a two-component therapy for Pompe disease.

What is the price predicton of BMRN Stock?

Wall Street analysts forecast BMRN stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for BMRN is87.35 USD with a low forecast of 60.00 USD and a high forecast of 120.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is BioMarin Pharmaceutical Inc (BMRN)'s revenue for the last quarter?

BioMarin Pharmaceutical Inc revenue for the last quarter amounts to 766.21M USD, increased 2.83

What is BioMarin Pharmaceutical Inc (BMRN)'s earnings per share (EPS) for the last quarter?

BioMarin Pharmaceutical Inc. EPS for the last quarter amounts to 0.54 USD, decreased -43.16

How many employees does BioMarin Pharmaceutical Inc (BMRN). have?

BioMarin Pharmaceutical Inc (BMRN) has 3221 emplpoyees as of June 03 2026.

What is BioMarin Pharmaceutical Inc (BMRN) market cap?

Today BMRN has the market capitalization of 10.31B USD.